ENST00000592092.2:n.553A>G
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|
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ENST00000673918.2:c.6181A>G
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ENSP00000501283.1:p.Thr2061Ala
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ENST00000674114.2:c.3788A>G
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ENSP00000501039.2:n.3788A>G
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|
ENST00000684977.1:c.1465A>G
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ENSP00000509384.1:p.Thr489Ala
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ENST00000689544.1:n.1400A>G
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|
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ENST00000691421.1:c.1468A>G
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ENSP00000508674.1:p.Thr490Ala
|
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ENST00000691855.1:c.5789A>G
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|
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ENST00000692961.1:c.6247A>G
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ENSP00000509289.1:p.Thr2083Ala
|
|
ENST00000693677.1:c.704+467A>G
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ENSP00000509779.1:n.704+467A>G
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ENST00000420124.4:c.6247A>G
MANE Select
|
ENSP00000398837.2:p.Thr2083Ala
|
|
ENST00000673918.1:c.6181A>G
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ENSP00000501283.1:p.Thr2061Ala
|
|
ENST00000674114.1:c.3569A>G
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|
|
ENST00000420124.2:c.6247A>G
|
ENSP00000398837.1:p.Thr2083Ala
|
|
NM_014727.2:c.6247A>G
|
NP_055542.1:p.Thr2083Ala
|
|
XM_011527561.1:c.6181A>G
|
XP_011525863.1:p.Thr2061Ala
|
|
XM_011527562.1:c.6247A>G
|
XP_011525864.1:p.Thr2083Ala
|
|
XM_011527563.1:c.5971A>G
|
XP_011525865.1:p.Thr1991Ala
|
|
XM_011527561.2:c.5683A>G
|
XP_011525863.2:p.Thr1895Ala
|
|
XM_011527562.2:c.6247A>G
|
XP_011525864.1:p.Thr2083Ala
|
|
XM_017027544.1:c.6247A>G
|
XP_016883033.1:p.Thr2083Ala
|
|
XM_017027545.1:c.5683A>G
|
XP_016883034.1:p.Thr1895Ala
|
|
XM_017027546.1:c.3211A>G
|
XP_016883035.1:p.Thr1071Ala
|
|
NM_014727.3:c.6247A>G
MANE Select
|
NP_055542.1:p.Thr2083Ala
|
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